MAUDE Adverse Event Report: RXSIGHT, INC. LIGHT ADJUSTABLE LENS+ (LAL+)

Model Number	60007
Medical Device Problem Code	Use of Device Problem (1670)
Health Effect - Clinical Code	Blurred Vision (2137)
Date of Event	12/04/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
A site reported to rxsight that a patient was bilaterally implanted with the light adjustable lens+ (lal+, sn (b)(6), +22.5d) in the left eye on (b)(6) 2024.Postoperatively, the patient completed 1 light adjustment in the left eye but delayed the lock in treatment due to dry eye treatment and light adjustment of the right eye.Upon examination on (b)(6) 2025, the treating physician observed central intraocular lens irregularities consistent with polymerization.Lock in treatment was performed on the same day.A procedure was attempted on (b)(6) 2025 to explant the lens, however, due to zonular dehiscence the procedure was not completed.On (b)(6) 2025, approximately 12 months after implantation, the lal+ was explanted and a new light adjustable lens (lal, sn (b)(6), +22.5d) implanted as a replacement.
Additional Manufacturer Narrative
The device history record for the manufacturing lot was reviewed and there were no discrepancies or unusual findings.Manufacturer reference #: (b)(4).

• Brand Name: LIGHT ADJUSTABLE LENS+ (LAL+)
• Common Device Name: LIGHT ADJUSTABLE LENS+ (LAL+)
• Manufacturer (Section D): RXSIGHT, INC.; 100 columbia; aliso viejo CA 92656
• Manufacturer (Section G): RXSIGHT, INC.; 100 columbia; aliso viejo CA 92656
• Manufacturer Contact: jim zhang ; 100 columbia; aliso viejo, CA 92656 ; 9492736163
• MDR Report Key: 23936879
• Report Number: 3012712027-2025-00454
• Device Sequence Number: 20236872
• Product Code: PZK
• UDI-Device Identifier: 00818806021637
• UDI-Public: 01008188060216371124020817270131
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: P160055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Device Explanted Year: 2025
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 12/31/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 60007
• Device Catalogue Number: 60007
• Device Lot Number: L08-005910
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/04/2025
• Initial Report FDA Received Date: 12/31/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 02/08/2024
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 69 YR
• Patient Sex: Female